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September 30, 2025Open Access

Network pharmacology, bioinformatics, molecular docking and experimental verification of the mechanism of HXZTS treatment on osteoarthritis synovium

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Authors

LCLi‐Qun ChenHWHongxiu WangDWDongzhi Wu

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Overview

Integration of network pharmacology and molecular docking reveals HXZTS targets inflammation in osteoarthritis, suggesting new therapeutic avenues.

Key Points

  • HXZTS treatment reduced inflammatory mediators IL6 and PTGS2 while promoting cartilage repair gene expression MMP1 and MMP3.
  • Network analysis identified 21 active ingredients and 111 targets associated with HXZTS, highlighting quercetin and β-sitosterol.
  • Molecular docking demonstrated strong binding affinities of HXZTS compounds with targets including AKT1, TNF, and TP53.
  • The multifaceted mechanism of HXZTS involves modulation of inflammation, oxidative stress, and metabolic pathways.

Cite This Study

Chen et al. (2025) studied this question.

synapsesocial.com/papers/68dc261d8a7d58c25ebb2b08https://doi.org/10.1101/2025.09.25.678423
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